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青蛙脊髓中氨基酸诱导及突触兴奋的二肽拮抗剂

Dipeptide antagonists of amino acid-induced and synaptic excitation in the frog spinal cord.

作者信息

Francis A A, Jones A W, Watkins J C

出版信息

J Neurochem. 1980 Dec;35(6):1458-60. doi: 10.1111/j.1471-4159.1980.tb09025.x.

Abstract

The dipeptide gamma-D-glutamylglycine (gamma DGG) antagonizes amino acid-induced depolarization and synaptic excitation in the isolated hemisected spinal cord of the frog. In general, the effects of this compound resembled those of the structurally similar D-alpha-aminosuberate (D alpha AS) in being more effective against N-methyl-D-aspartate (NMDA)-induced responses than against responses induced by other excitatory amino acids. However gamma DGG appeared to be more effective than D alpha AS in depressing kainate-induced responses. Similar, though weaker, effects were produced by the L isomer of the dipeptide (gamma LGG), a natural brain constituent.

摘要

二肽γ-D-谷氨酰甘氨酸(γ-DGG)可拮抗青蛙离体半切脊髓中氨基酸诱导的去极化和突触兴奋。一般来说,该化合物的作用与结构相似的D-α-氨基辛酸盐(D-α-AS)类似,对N-甲基-D-天冬氨酸(NMDA)诱导的反应比对其他兴奋性氨基酸诱导的反应更有效。然而,γ-DGG在抑制红藻氨酸诱导的反应方面似乎比D-α-AS更有效。二肽的L异构体(γ-LGG)是一种天然脑成分,也产生了类似但较弱的作用。

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